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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 232 (1971), S. 327-330 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Our studies were designed to discover the fate of oleic acid in an aquatic sediment. The basis of our experiments was to add 9,10-3H, l-14C-oleic acid to the upper layers of the Recent sediments of the Severn Estuary and then to isolate the labelled products of short term diagenesis. The ratios of ...
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Mass spectra of trimethylsilyl (TMS) derivatives of long chain dicarboxylic acids, hydroxy acids, cyano acids, and terminal diols, dithiols and diamines have been examined. A number of fragmentation pathways involving rearrangement of partial or intact TMS groups between the termini or remote points in the chain have been determined, using deuterium and carbon-13 labeling, and high resolution mass spectrometry. Knowledge of the occurrence of functional group migrations of this type is essential to the correct interpretation of mass spectra of TMS derivatives, which are now in wide use in mass spectrometry and gas chromatography. These data in addition provide further evidence for the general ability of remote functional groups to interact, by winding or coiling of long chains. A number of interesting doubly-charged ions are reported, in which the charges are reported, in which the charges are located at opposite ends of long chains, and for which no singly-charged counterparts are observed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 3 (1970), S. 399-401 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Some of the observed fragmentation reactions of long-chain aliphatic methoxyesters necessitate the interaction of both functional groups, even when these are located far apart: both alcohol eliminations from the ion formed by α-cleavage to the ether function which contains the ester group are highly specific: they involve a hydrogen atom in the position adjacent to the methoxyl-bearing carbon.
    Notes: Certaines des fragmentations des méthoxyesters aliphatiques à longue chaíne nécessitent l'interation des deux fonctions: les deux éliminations d'alcool que subit l'ion par rupture en α de la fanction éther et comprenant le groupe ester, sont trés spécifiques: elles mettent en cause un atome d'hydrogéne en position adjacente au carbone qui porte le groupe méthoxyle.
    Type of Medium: Electronic Resource
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